ClearanceBrief
510(k) K833892 ยท GGP Test, Qualitative And Quantitative Factor Deficiency

COATEST FACTOR VIII

ApplicantKabivitrum, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jan 30, 1984
ReceivedNov 9, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833892

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.